ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.1350-75_1492del

dbSNP: rs1577195893
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust RCV000787270 SCV000926197 pathogenic Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 2019-05-03 no assertion criteria provided clinical testing

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